Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP674622.RAQLLwxZciORhyzB7jfmLWwSQavAMLMTDrjZ8GeGt8Tzw130_assertion> ?p ?o ?g. }
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- NP674622.RAQLLwxZciORhyzB7jfmLWwSQavAMLMTDrjZ8GeGt8Tzw130_assertion type Assertion NP674622.RAQLLwxZciORhyzB7jfmLWwSQavAMLMTDrjZ8GeGt8Tzw130_head.
- NP674622.RAQLLwxZciORhyzB7jfmLWwSQavAMLMTDrjZ8GeGt8Tzw130_assertion description "[These data provide a proof-of-concept that the catalogue of p63 binding sites identified in this study may be of relevance to the studies of SHFM and other congenital malformations that resemble the p63-associated phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674622.RAQLLwxZciORhyzB7jfmLWwSQavAMLMTDrjZ8GeGt8Tzw130_provenance.
- NP674622.RAQLLwxZciORhyzB7jfmLWwSQavAMLMTDrjZ8GeGt8Tzw130_assertion evidence source_evidence_literature NP674622.RAQLLwxZciORhyzB7jfmLWwSQavAMLMTDrjZ8GeGt8Tzw130_provenance.
- NP674622.RAQLLwxZciORhyzB7jfmLWwSQavAMLMTDrjZ8GeGt8Tzw130_assertion SIO_000772 20808887 NP674622.RAQLLwxZciORhyzB7jfmLWwSQavAMLMTDrjZ8GeGt8Tzw130_provenance.
- NP674622.RAQLLwxZciORhyzB7jfmLWwSQavAMLMTDrjZ8GeGt8Tzw130_assertion wasDerivedFrom befree-20150227 NP674622.RAQLLwxZciORhyzB7jfmLWwSQavAMLMTDrjZ8GeGt8Tzw130_provenance.
- NP674622.RAQLLwxZciORhyzB7jfmLWwSQavAMLMTDrjZ8GeGt8Tzw130_assertion wasGeneratedBy ECO_0000203 NP674622.RAQLLwxZciORhyzB7jfmLWwSQavAMLMTDrjZ8GeGt8Tzw130_provenance.